Velasco Riccardo, Zharkikh Andrey, Troggio Michela, Cartwright Dustin A, Cestaro Alessandro, Pruss Dmitry, Pindo Massimo, Fitzgerald Lisa M, Vezzulli Silvia, Reid Julia, Malacarne Giulia, Iliev Diana, Coppola Giuseppina, Wardell Bryan, Micheletti Diego, Macalma Teresita, Facci Marco, Mitchell Jeff T, Perazzolli Michele, Eldredge Glenn, Gatto Pamela, Oyzerski Rozan, Moretto Marco, Gutin Natalia, Stefanini Marco, Chen Yang, Segala Cinzia, Davenport Christine, Demattè Lorenzo, Mraz Amy, Battilana Juri, Stormo Keith, Costa Fabrizio, Tao Quanzhou, Si-Ammour Azeddine, Harkins Tim, Lackey Angie, Perbost Clotilde, Taillon Bruce, Stella Alessandra, Solovyev Victor, Fawcett Jeffrey A, Sterck Lieven, Vandepoele Klaas, Grando Stella M, Toppo Stefano, Moser Claudio, Lanchbury Jerry, Bogden Robert, Skolnick Mark, Sgaramella Vittorio, Bhatnagar Satish K, Fontana Paolo, Gutin Alexander, Van de Peer Yves, Salamini Francesco, Viola Roberto
IASMA Research Center, San Michele all'Adige, Trento, Italy.
PLoS One. 2007 Dec 19;2(12):e1326. doi: 10.1371/journal.pone.0001326.
Worldwide, grapes and their derived products have a large market. The cultivated grape species Vitis vinifera has potential to become a model for fruit trees genetics. Like many plant species, it is highly heterozygous, which is an additional challenge to modern whole genome shotgun sequencing. In this paper a high quality draft genome sequence of a cultivated clone of V. vinifera Pinot Noir is presented.
We estimate the genome size of V. vinifera to be 504.6 Mb. Genomic sequences corresponding to 477.1 Mb were assembled in 2,093 metacontigs and 435.1 Mb were anchored to the 19 linkage groups (LGs). The number of predicted genes is 29,585, of which 96.1% were assigned to LGs. This assembly of the grape genome provides candidate genes implicated in traits relevant to grapevine cultivation, such as those influencing wine quality, via secondary metabolites, and those connected with the extreme susceptibility of grape to pathogens. Single nucleotide polymorphism (SNP) distribution was consistent with a diffuse haplotype structure across the genome. Of around 2,000,000 SNPs, 1,751,176 were mapped to chromosomes and one or more of them were identified in 86.7% of anchored genes. The relative age of grape duplicated genes was estimated and this made possible to reveal a relatively recent Vitis-specific large scale duplication event concerning at least 10 chromosomes (duplication not reported before).
Sanger shotgun sequencing and highly efficient sequencing by synthesis (SBS), together with dedicated assembly programs, resolved a complex heterozygous genome. A consensus sequence of the genome and a set of mapped marker loci were generated. Homologous chromosomes of Pinot Noir differ by 11.2% of their DNA (hemizygous DNA plus chromosomal gaps). SNP markers are offered as a tool with the potential of introducing a new era in the molecular breeding of grape.
在全球范围内,葡萄及其衍生产品拥有庞大的市场。栽培葡萄品种欧亚葡萄有潜力成为果树遗传学的一个模型。与许多植物物种一样,它高度杂合,这对现代全基因组鸟枪法测序来说是一个额外的挑战。本文展示了欧亚葡萄黑比诺栽培克隆的高质量基因组草图序列。
我们估计欧亚葡萄的基因组大小为504.6兆碱基对。对应于477.1兆碱基对的基因组序列被组装成2093个元重叠群,435.1兆碱基对被定位到19个连锁群(LGs)上。预测基因的数量为29585个,其中96.1%被分配到连锁群上。葡萄基因组的这种组装提供了与葡萄栽培相关性状有关的候选基因,例如那些通过次生代谢物影响葡萄酒质量的基因,以及那些与葡萄对病原体的极端易感性相关的基因。单核苷酸多态性(SNP)分布与全基因组的弥散单倍型结构一致。在大约200万个SNP中,1751176个被定位到染色体上,并且在86.7%的定位基因中鉴定出了其中一个或多个。估计了葡萄重复基因的相对年龄,这使得揭示至少涉及10条染色体的相对较新的葡萄特异性大规模复制事件(之前未报道过的复制)成为可能。
桑格鸟枪法测序和高效的合成测序(SBS),以及专门的组装程序,解析了一个复杂的杂合基因组。生成了基因组的一致序列和一组定位的标记位点。黑比诺的同源染色体在其DNA(半合子DNA加上染色体间隙)上有11.2%的差异。SNP标记作为一种工具被提供,有潜力在葡萄分子育种中引入一个新时代。